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Mucosal Melanoma of Eustachian Tube: A Case Report

Mucosal melanoma originating from the eustachian tube is very rare, and only 15 cases were reported so far. In this study, we report a case of mucosal melanoma from the eustachian tube which was surgically managed, followed by chemoradiotherapy. A 53-year-old man presented with a history of recurren...

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Autores principales: Jee Kang, Yung, Bum Kim, Min, Duk Hong, Sang, Cho, Yang-Sun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Academy of Otology and Neurotology and the Politzer Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524376/
https://www.ncbi.nlm.nih.gov/pubmed/36063100
http://dx.doi.org/10.5152/iao.2022.21573
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author Jee Kang, Yung
Bum Kim, Min
Duk Hong, Sang
Cho, Yang-Sun
author_facet Jee Kang, Yung
Bum Kim, Min
Duk Hong, Sang
Cho, Yang-Sun
author_sort Jee Kang, Yung
collection PubMed
description Mucosal melanoma originating from the eustachian tube is very rare, and only 15 cases were reported so far. In this study, we report a case of mucosal melanoma from the eustachian tube which was surgically managed, followed by chemoradiotherapy. A 53-year-old man presented with a history of recurrent idiopathic hemotympanum and a dark red mass in the nasopharynx protruding from the eustachian tube orifice. Under an impression of mucosal melanoma from the eustachian tube, en-bloc surgical removal was performed using the infratemporal fossa approach type C combined with a transnasal endoscopic approach followed by postoperative chemoradiotherapy. However, the disease progressed to lung metastasis, and the patient died of the disease at 13 months postoperatively. The presenting case showed a poor progression despite a ­margin-free surgical resection followed by chemoradiotherapy. Additional trial of new treatment options is necessary to improve the poor prognosis.
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spelling pubmed-95243762022-10-13 Mucosal Melanoma of Eustachian Tube: A Case Report Jee Kang, Yung Bum Kim, Min Duk Hong, Sang Cho, Yang-Sun J Int Adv Otol Case Report Mucosal melanoma originating from the eustachian tube is very rare, and only 15 cases were reported so far. In this study, we report a case of mucosal melanoma from the eustachian tube which was surgically managed, followed by chemoradiotherapy. A 53-year-old man presented with a history of recurrent idiopathic hemotympanum and a dark red mass in the nasopharynx protruding from the eustachian tube orifice. Under an impression of mucosal melanoma from the eustachian tube, en-bloc surgical removal was performed using the infratemporal fossa approach type C combined with a transnasal endoscopic approach followed by postoperative chemoradiotherapy. However, the disease progressed to lung metastasis, and the patient died of the disease at 13 months postoperatively. The presenting case showed a poor progression despite a ­margin-free surgical resection followed by chemoradiotherapy. Additional trial of new treatment options is necessary to improve the poor prognosis. European Academy of Otology and Neurotology and the Politzer Society 2022-09-01 /pmc/articles/PMC9524376/ /pubmed/36063100 http://dx.doi.org/10.5152/iao.2022.21573 Text en 2022 authors https://creativecommons.org/licenses/by-nc/4.0/ Content of this journal is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle Case Report
Jee Kang, Yung
Bum Kim, Min
Duk Hong, Sang
Cho, Yang-Sun
Mucosal Melanoma of Eustachian Tube: A Case Report
title Mucosal Melanoma of Eustachian Tube: A Case Report
title_full Mucosal Melanoma of Eustachian Tube: A Case Report
title_fullStr Mucosal Melanoma of Eustachian Tube: A Case Report
title_full_unstemmed Mucosal Melanoma of Eustachian Tube: A Case Report
title_short Mucosal Melanoma of Eustachian Tube: A Case Report
title_sort mucosal melanoma of eustachian tube: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524376/
https://www.ncbi.nlm.nih.gov/pubmed/36063100
http://dx.doi.org/10.5152/iao.2022.21573
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